A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670869



Internal ID9936974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63026408..63026701hg38UCSC Ensembl
chr20:61657760..61658053hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6291285, essv5741099, essv6325274, essv5406217, essv6555795
SamplesNA19087, NA18945, HG00607, NA18989, NA18620
Known GenesLOC63930
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670869
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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